Connecticut Diagnostics, Ltd.
Connecticut Diagnostics, Ltd. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1991.
Top product codes for Connecticut Diagnostics, Ltd.
Recent clearances by Connecticut Diagnostics, Ltd.
- K905617 — VISI-STAPH
- K822500 — CDL LYSING REAGENT
- K822501 — CDL ISOTONIC DILUENT
- K822504 — CDL AUTO-LYSING REAGENT
- K811222 — INORGANIC PHOSPHORUS REAGENTS
- K801897 — GLUCOSE DIAGNOSTIC REAGENT
- K801898 — URIC ACID DIAGNOSTIC REAGENT
- K792465 — CONNECTICUT DIAGNOSTICS, LTS. DIRECT
- K792337 — DONNECT. DIAG. CALCIUM DIAG. REAGENT
- K792338 — DONNECT. DIAG. TOTAL BILIRUBIN REAGENTS
- K792339 — CONNECT. DIAG. ALBUMIN DIAGNOSTIC REAGEN
- K792340 — CONNECT. DIAG. TOTAL PROTEIN DIAG. REAGE
- K792362 — BLOOD UREA NITROGEN REAGENT
- K791994 — CREATININE DIAG. REAGENT PICRIC ACID
Data sourced from openFDA. This site is unofficial and independent of the FDA.